Genome-wide discovery of human splicing branchpoints [BPCapture]
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Genome-wide discovery of human splicing branchpoints [BPCapture]
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2014-10-01
相关数据集
Regulation of constitutive and alternative messenger RNA splicing across the human transcriptome by PRPF8 is determined by 5' splice site strength. Regulation of constitutive and alternative messenger RNA splicing across the human transcriptome by PRPF8 is determined by 5' splice site strength
RNA-sequencing experiments performed on control siRNA treated and PRPF8 depleted cells
NIAID Data Ecosystem80
Genome location of the top 48 up-regulated genes in synMuv B mutants as well as Orsay virus infected wild type map to a few clusters in the genome.
Genome location of the top 48 up-regulated genes in synMuv B mutants as well as Orsay virus infected wild type map to a few clusters in the genome.
Figshare2025-01-29 更新40
Size and structure of five resistance gene analogs and their mapping to chromosome 0 of C . canephora genome.
Size and structure of five resistance gene analogs and their mapping to chromosome 0 of C. canephora genome.
NIAID Data Ecosystem20
The impact of Prp18p on splicing fidelity and efficiency in budding yeast
Fidelity of 3´-splice site (3´SS) selection by the spliceosome is critical for proper gene expression but is a daunting task considering the low complexity of the 3´SS consensus YAG. Here we show that
Alliance of Genome Resources40
An uncharacterized gene, C7orf26, identified from an autosomal dominant ocular disease functions in mRNA splicing. An uncharacterized gene, C7orf26, identified from an autosomal dominant ocular disease functions in mRNA splicing
An uncharacterized gene, C7orf26 was expected to function with the integrator complex in mRNA splicing. To address the involvement of mRNA splicing, we performed microarray analysis of HeLa/C7orf26 si
NIAID Data Ecosystem30
